The efficacy and safety of anti-Aβ agents for delaying cognitive decline in Alzheimer's disease: a meta-analysis

被引:5
|
作者
Li, Jiaxuan [1 ,2 ]
Wu, Xin [1 ,2 ]
Tan, Xin [3 ]
Wang, Shixin [1 ,2 ]
Qu, Ruisi [1 ,2 ]
Wu, Xiaofeng [4 ]
Chen, Zhouqing [1 ,2 ]
Wang, Zhong [1 ,2 ]
Chen, Gang [1 ,2 ]
机构
[1] Soochow Univ, Dept Neurosurgery, Affiliated Hosp 1, Suzhou, Jiangsu, Peoples R China
[2] Soochow Univ, Brain & Nerve Res Lab, Affiliated Hosp 1, Suzhou, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Suzhou Municipal Hosp, Affiliated Suzhou Hosp, Dept Neurol, Suzhou, Jiangsu, Peoples R China
[4] Soochow Univ, Dept Ultrasound, Affiliated Hosp 1, Suzhou, Jiangsu, Peoples R China
来源
关键词
Alzheimer's disease; cognitive impairment; amyloid-beta; monoclonal antibody; gamma-secretase inhibitors; BACE-1; inhibitors; intravenous immunoglobulin; gamma-secretase modulators; GAMMA-SECRETASE INHIBITORS; IMMUNOTHERAPY; MODULATORS;
D O I
10.3389/fnagi.2023.1257973
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background: This meta-analysis evaluates the efficacy and safety of amyloid-beta (A beta) targeted therapies for delaying cognitive deterioration in Alzheimer's disease (AD).Methods: PubMed, EMBASE, the Cochrane Library, and ClinicalTrials.gov were systematically searched to identify relevant studies published before January 18, 2023.Results: We pooled 33,689 participants from 42 studies. The meta-analysis showed no difference between anti-A beta drugs and placebo in the Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog), and anti-A beta drugs were associated with a high risk of adverse events [ADAS-Cog: MDs = -0.08 (-0.32 to 0.15), p = 0.4785; AEs: RR = 1.07 (1.02 to 1.11), p = 0.0014]. Monoclonal antibodies outperformed the placebo in delaying cognitive deterioration as measured by ADAS-Cog, Clinical Dementia Rating-Sum of Boxes (CDR-SB), Mini-Mental State Examination (MMSE) and Alzheimer's Disease Cooperative Study-Activities of Daily Living (ADCS-ADL), without increasing the risk of adverse events [ADAS-Cog: MDs = -0.55 (-0.89 to 0.21), p = 0.001; CDR-SB: MDs = -0.19 (-0.29 to -0.10), p < 0.0001; MMSE: MDs = 0.19 (0.00 to 0.39), p = 0.05; ADCS-ADL: MDs = 1.26 (0.84 to 1.68), p < 0.00001]. Intravenous immunoglobulin and gamma-secretase modulators (GSM) increased cognitive decline in CDR-SB [MDs = 0.45 (0.17 to 0.74), p = 0.002], but had acceptable safety profiles in AD patients. gamma-secretase inhibitors (GSI) increased cognitive decline in ADAS-Cog, and also in MMSE and ADCS-ADL. BACE-1 inhibitors aggravated cognitive deterioration in the outcome of the Neuropsychiatric Inventory (NPI). GSI and BACE-1 inhibitors caused safety concerns. No evidence indicates active A beta immunotherapy, MPAC, or tramiprosate have effects on cognitive function and tramiprosate is associated with serious adverse events.Conclusion: Current evidence does not show that anti-A beta drugs have an effect on cognitive performance in AD patients. However, monoclonal antibodies can delay cognitive decline in AD. Development of other types of anti-A beta drugs should be cautious.
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页数:12
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